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For: Fu L, Liu Y, Wan JP. Pd-Catalyzed Triple-Fold C(sp2)-H Activation with Enaminones and Alkenes for Pyrrole Synthesis via Hydrogen Evolution. Org Lett 2021;23:4363-7. [PMID: 34013729 DOI: 10.1021/acs.orglett.1c01301] [Cited by in Crossref: 26] [Cited by in F6Publishing: 30] [Article Influence: 13.0] [Reference Citation Analysis]
Number Citing Articles
1 Liu D, Song S, Chen L, Zhang M, Liu Z, Lu X, Huang J, Yu F. Access to thiionized-, selenolized-, and alkylated 5-alkylidene 3-pyrrolin-2-one derivatives via a regioselective oxidative annulation reaction. Org Biomol Chem 2023;21:2596-602. [PMID: 36891944 DOI: 10.1039/d3ob00014a] [Reference Citation Analysis]
2 Molnár Á. Recent Advances in the Synthesis of Five‐membered Nitrogen Heterocycles Induced by Palladium Ions and Complexes. ChemistrySelect 2023;8. [DOI: 10.1002/slct.202300153] [Reference Citation Analysis]
3 Zhou C, Zheng H, Chen Y, Mao G, Deng GJ. Modular Synthesis of Tetrasubstituted Pyrroles through a Four-Component Cyclization Strategy Using Ammonium Salt as the Nitrogen Source. J Org Chem 2023;88:1533-44. [PMID: 36655334 DOI: 10.1021/acs.joc.2c02556] [Reference Citation Analysis]
4 Zhao B, Li H, Jiang F, Wan JP, Cheng K, Liu Y. Synergistic Visible Light and Pd-Catalyzed C-H Alkylation of 1-Naphthylamines with α-Diazoesters. J Org Chem 2023;88:640-6. [PMID: 36538361 DOI: 10.1021/acs.joc.2c01702] [Reference Citation Analysis]
5 Lopchuk JM. Five-membered ring systems: pyrroles and benzo analogs. Progress in Heterocyclic Chemistry 2023. [DOI: 10.1016/b978-0-443-18939-5.00006-8] [Reference Citation Analysis]
6 Liu N, Cuan X, Li H, Duan X. Progress in the Study of α-Functionalization of Enaminone. Chinese Journal of Organic Chemistry 2023;43:602. [DOI: 10.6023/cjoc202207027] [Reference Citation Analysis]
7 Lu MZ, Goh J, Maraswami M, Jia Z, Tian JS, Loh TP. Recent Advances in Alkenyl sp(2) C-H and C-F Bond Functionalizations: Scope, Mechanism, and Applications. Chem Rev 2022;122:17479-646. [PMID: 36240299 DOI: 10.1021/acs.chemrev.2c00032] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
8 Leung MP, Tsang YL, Choy PY, Kwong FY. Recent Advances in Palladium‐Based Cross‐Dehydrogenative‐Coupling (CDC) with C(sp 2 )H/C(sp 2 )H Bond to Form New C(sp 2 )C(sp 2 ) Bond. Handbook of CH‐Functionalization 2022. [DOI: 10.1002/9783527834242.chf0157] [Reference Citation Analysis]
9 Lv K, Zhao Q, Zhao K, Yang J, Yan S. Cu-Catalyzed Oxidative [3 + 2] Annulation of 2-(Pyridine-2-yl)acetates with Maleimides: Synthesis of 1H-Pyrrolo[3,4-b]indolizine-1,3-diones. J Org Chem 2022;87:15301-15311. [DOI: 10.1021/acs.joc.2c01879] [Reference Citation Analysis]
10 Cheng D, Yang H, Yu C, Tao Y, Xu X. Synthesis of Multi-arylated Pyridines via Tandem Oxidative Reaction. Tetrahedron Letters 2022. [DOI: 10.1016/j.tetlet.2022.154243] [Reference Citation Analysis]
11 Duan X, Liu K, Meng Z, Guo Y, Li H, Liu N, Qu W, Duan X, Ma J. 1,3-Dibromo-5, 5-dimethylhydantoin (DBDMH)-promoted cross-coupling of enaminones with phenols under metal-free conditions. Tetrahedron Letters 2022. [DOI: 10.1016/j.tetlet.2022.154111] [Reference Citation Analysis]
12 Mengxin X, Lambu MR, Judeh ZMA. Selective One-Pot Cascade Synthesis of N-Substituted Highly Functionalized Pyrroles from Unprotected Sugars, Primary Amines, and Oxoacetonitriles. J Org Chem 2022. [PMID: 36044395 DOI: 10.1021/acs.joc.2c01270] [Reference Citation Analysis]
13 Lu P, Zhuang W, Lu L, Liu A, Chen Y, Wu C, Zhang X, Huang Q. Chemodivergent Synthesis of Indeno[1,2-b]indoles and Isoindolo[2,1-a]indoles via Mn(III)-Mediated or Electrochemical Intramolecular Radical Cross-Dehydrogenative Coupling. J Org Chem 2022. [PMID: 35901234 DOI: 10.1021/acs.joc.2c01238] [Reference Citation Analysis]
14 Qiao S, Deng W, Deng G, Liang Y, Yang Y. Research advances in palladium-catalysed intermolecular C-H annulation of aryl halides with various aromatic ring precursors. Org Biomol Chem 2022. [PMID: 35861153 DOI: 10.1039/d2ob01129h] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
15 Hu X, Tao M, Ma Z, Zhang Y, Li Y, Liang D. Regioselective Photocatalytic Dialkylation/Cyclization Sequence of 3‐Aza‐1,5‐dienes: Access to 3,4‐Dialkylated 4‐Pyrrolin‐2‐ones. Adv Synth Catal. [DOI: 10.1002/adsc.202200183] [Reference Citation Analysis]
16 Shi T, Yin G, Wang X, Xiong Y, Peng Y, Li S, Zeng Y, Wang Z. Recent advances in the syntheses of pyrroles. Green Synthesis and Catalysis 2022. [DOI: 10.1016/j.gresc.2022.06.004] [Reference Citation Analysis]
17 Liu Y, Zhang T, Wan JP. Ultrasound-Promoted Synthesis of α-Thiocyanoketones via Enaminone C═C Bond Cleavage and Tunable One-Pot Access to 4-Aryl-2-aminothiazoles. J Org Chem 2022. [PMID: 35616657 DOI: 10.1021/acs.joc.2c00708] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
18 Xu Z, Geng X, Cai Y, Wang L. A Straightforward Approach to Fluorinated Pyrimido[1,2-b]indazole Derivatives via Metal/Additive-Free Annulation with Enaminones, 3-Aminoindazoles, and Selectfluor. J Org Chem 2022. [PMID: 35486919 DOI: 10.1021/acs.joc.2c00136] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
19 Wang Z, Zhao B, Liu Y, Wan J. Recent Advances in Reactions Using Enaminone in Water or Aqueous Medium. Adv Synth Catal 2022;364:1508-21. [DOI: 10.1002/adsc.202200144] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 7.0] [Reference Citation Analysis]
20 Wu CC, Ambre R, Lee MH, Shie JJ. Flexible Construction Approach to the Synthesis of 1,5-Substituted Pyrrole-3-carbaldehydes from 5-Bromo-1,2,3-triazine. Org Lett 2022. [PMID: 35385278 DOI: 10.1021/acs.orglett.2c00891] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
21 Sahoo AK, Rakshit A, Dahiya A, Pan A, Patel BK. Visible-Light-Mediated Synthesis of Thio-Functionalized Pyrroles. Org Lett . [DOI: 10.1021/acs.orglett.2c00283] [Cited by in Crossref: 7] [Cited by in F6Publishing: 9] [Article Influence: 7.0] [Reference Citation Analysis]
22 Nakamura M, Yoshida K, Togo H. Novel preparation of 2,5-diarylpyrroles from aromatic nitriles with 3-arylpropylmagnesium bromides, 1,3-diiodo-5,5-dimethylhydantoin, and BuOK. Tetrahedron 2022. [DOI: 10.1016/j.tet.2022.132709] [Reference Citation Analysis]
23 Ge D, Sun LW, Yu ZL, Luo XL, Xu P, Shen ZL. Regioselective synthesis of 6-nitroindole derivatives from enaminones and nitroaromatic compounds via transition metal-free C-C and C-N bond formation. Org Biomol Chem 2022. [PMID: 35107115 DOI: 10.1039/d1ob02443d] [Reference Citation Analysis]
24 Guo Y, Liu Y, Wan J. Amine-catalyzed synthesis of N2-sulfonyl 1,2,3-triazole in water and the tunable N2-H 1,2,3-triazole synthesis in DMSO via metal-free enamine annulation. Chinese Chemical Letters 2022;33:855-8. [DOI: 10.1016/j.cclet.2021.08.003] [Cited by in Crossref: 7] [Cited by in F6Publishing: 8] [Article Influence: 7.0] [Reference Citation Analysis]
25 Dong L, Zhang S, Zhang W, Dong Y, Mo L, Zhang Z. Synthesis, characterization and application of magnetic biochar sulfonic acid as a highly efficient recyclable catalyst for preparation of spiro-pyrazolo[3,4-b]pyridines. Res Chem Intermed. [DOI: 10.1007/s11164-022-04660-6] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
26 Xia XF, Niu YN. Recent developments in the synthesis of nitrogen-containing heterocycles from β-aminovinyl esters/ketones as CC-N donors. Org Biomol Chem 2022;20:282-95. [PMID: 34877952 DOI: 10.1039/d1ob01998h] [Cited by in Crossref: 10] [Cited by in F6Publishing: 12] [Article Influence: 10.0] [Reference Citation Analysis]
27 Liu D, Lu X, Zhang Q, Zhao Y, Zhang B, Sun Y, Dai W, Xu Y, Yu F. Facile approach to multifunctionalized 5-alkylidene-3-pyrrolin-2-ones via regioselective oxidative cyclization of 2,4-pentanediones with primary amines and sodium sulfinates. Org Chem Front . [DOI: 10.1039/d2qo00473a] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
28 He J, Yang Z, Zhou X, Li Y, Gao S, Shi L, Liang D. Exploring the regioselectivity of the cyanoalkylation of 3-aza-1,5-dienes: photoinduced synthesis of 3-cyanoalkyl-4-pyrrolin-2-ones. Org Chem Front . [DOI: 10.1039/d2qo00918h] [Reference Citation Analysis]
29 Guo H, Liu Y, Wen C, Wan J. Electrochemical enaminone C–H thiolation/C–N amination cascade for thiazole synthesis and its diastereoselective dearomatization. Green Chem . [DOI: 10.1039/d2gc01644c] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
30 Guo H, Tian L, Liu Y, Wan JP. DMSO as a C1 Source for [2 + 2 + 1] Pyrazole Ring Construction via Metal-Free Annulation with Enaminones and Hydrazines. Org Lett 2021. [PMID: 34908420 DOI: 10.1021/acs.orglett.1c03879] [Cited by in Crossref: 15] [Cited by in F6Publishing: 20] [Article Influence: 7.5] [Reference Citation Analysis]
31 Wen S, Tian Q, Chen Y, Zhang Y, Cheng G. Annulation of CF3-Imidoyl Sulfoxonium Ylides with 1,3-Dicarbonyl Compounds: Access to 1,2,3-Trisubstituted 5-Trifluoromethylpyrroles. Org Lett 2021;23:7407-11. [PMID: 34543038 DOI: 10.1021/acs.orglett.1c02598] [Cited by in Crossref: 6] [Cited by in F6Publishing: 10] [Article Influence: 3.0] [Reference Citation Analysis]
32 Liu T, Wan JP, Liu Y. Metal-free enaminone C-N bond cyanation for the stereoselective synthesis of (E)- and (Z)-β-cyano enones. Chem Commun (Camb) 2021;57:9112-5. [PMID: 34498638 DOI: 10.1039/d1cc03292e] [Cited by in Crossref: 16] [Cited by in F6Publishing: 17] [Article Influence: 8.0] [Reference Citation Analysis]
33 Lin Y, Jin J, Wang C, Wan JP, Liu Y. Electrochemical C-H Halogenations of Enaminones and Electron-Rich Arenes with Sodium Halide (NaX) as Halogen Source for the Synthesis of 3-Halochromones and Haloarenes. J Org Chem 2021;86:12378-85. [PMID: 34392684 DOI: 10.1021/acs.joc.1c01347] [Cited by in Crossref: 14] [Cited by in F6Publishing: 16] [Article Influence: 7.0] [Reference Citation Analysis]
34 Duan X, Li H, Li W, Wang J, Liu N. NBS‐Promoted C−H Amination of Enaminones for the Synthesis of N‐Heterocycle Substituted Enaminones**. ChemistrySelect 2021;6:6478-82. [DOI: 10.1002/slct.202101726] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]